Charles A Gersbach

Durham, NC, United States of America

Charles A Gersbach

USPTO Granted Patents = 19 

 

Average Co-Inventor Count = 2.6

ph-index = 9

Forward Citations = 159(Granted Patents)


Company Filing History:


Years Active: 2017-2025

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19 patents (USPTO):Explore Patents

Title: Charles A. Gersbach: Pioneering Gene Editing Innovator

Introduction: Charles A. Gersbach is a renowned inventor based in Durham, NC, who has made significant contributions to the field of gene editing. With a total of 18 patents to his name, he has been at the forefront of innovations targeting genetic diseases, particularly through advanced therapeutic applications.

Latest Patents: Among his most recent groundbreaking patents are "Therapeutic Targets for the Correction of the Human Dystrophin Gene by Gene Editing and Methods of Use," which focuses on innovative strategies for correcting the dystrophin gene responsible for muscular dystrophies. Additionally, his work on "Therapeutic Applications of CPF1-Based Genome Editing" emphasizes the versatility of the CRISPR/Cpf1 technology in medical applications, further enhancing the field of gene therapy.

Career Highlights: Gersbach has had an illustrious career, greatly influenced by his roles at prestigious institutions like Duke University and North Carolina State University. His research has not only pushed the boundaries of genetic engineering but has also opened new avenues for therapeutic interventions in genetic disorders.

Collaborations: Throughout his career, Gersbach has collaborated with notable professionals in the field, including Isaac B. Hilton and David G. Ousterout. These collaborations have further enriched his research, leading to innovative solutions in gene editing and therapy.

Conclusion: Charles A. Gersbach stands out as a pivotal figure in gene editing innovation. His contributions through numerous patents and collaborations reflect his dedication to advancing medical science and improving the lives of those affected by genetic disorders. As he continues to explore new frontiers in this vital area, his work is expected to have lasting impacts on the future of gene therapy.

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